Amyl 2-hydroxyethyl sulfide

Base Information

• Chemical Name: Amyl 2-hydroxyethyl sulfide
• CAS No.: 22812-91-5
• Molecular Formula: C₇H₁₆OS
• Molecular Weight: 148.269
• Hs Code.: 2930909090
• European Community (EC) Number: 654-553-3
• NSC Number: 84164
• DSSTox Substance ID: DTXSID60945488
• Nikkaji Number: J1.906.732G
• Wikidata: Q82922847
• Mol file: 22812-91-5.mol

Synonyms:2-pentylsulfanylethanol;22812-91-5;AMYL 2-HYDROXYETHYL SULFIDE;2-(n-Pentylthio)ethanol;26901-96-2;2-(Pentylsulfanyl)ethan-1-ol;2-Hydroxyethyl N-Amyl Sulfide;NSC84164;2-HYDROXYETHYL N-PENTYL SULFIDE;2-n-pentylthio-ethanol;2-(pentylsulfanyl)ethanol;2-(Pentylthio)ethan-1-ol;SCHEMBL1148304;DTXSID60945488;GMCYCIFSAJJFSY-UHFFFAOYSA-N;(+)-DI-TERT-BUTYLL-TARTRATE;MFCD00014043;NSC-84164;STK675267;2-(PENTYLSULFANYL)-1-ETHANOL;AKOS005593633;CS-0336330;FT-0612599

Chemical Property of Amyl 2-hydroxyethyl sulfide

Chemical Property:

• Boiling Point: 237.3°Cat760mmHg
• Flash Point: 116°C
• PSA: 45.53000
• Density: 0.953g/cm³
• LogP: 1.90210
• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 148.09218630
• Heavy Atom Count: 9
• Complexity: 48.2

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCSCCO

Technology Process of Amyl 2-hydroxyethyl sulfide

There total 3 articles about Amyl 2-hydroxyethyl sulfide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

n-pentanethiol (110-66-7) + 2-chloro-ethanol (107-07-3) → (2-Hydroxyethyl)-pentylsulfid (22812-91-5)

Guidance literature:

Multistep reaction; (i) aq. NaOH, benzene, (ii) /BRN= 878139/;

Reference yield:

amyl iodide (628-17-1) + 2-hydroxyethanethiol (60-24-2) → (2-Hydroxyethyl)-pentylsulfid (22812-91-5)

Guidance literature:

With sodium methylate; In methanol;

Reference yield:

→ (2-Hydroxyethyl)-pentylsulfid (22812-91-5)

Guidance literature:

2-Chlorethanol-(1), Pentylmercaptan, NaOH;

upstream raw materials:

amyl iodide

2-hydroxyethanethiol

n-pentanethiol

2-chloro-ethanol

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